Skip to main content
. Author manuscript; available in PMC: 2014 Jul 6.
Published in final edited form as: Shock. 2010 Feb;33(2):197–204. doi: 10.1097/SHK.0b013e3181ae8155

Figure 4. Adam17 levels in primary alveolar macrophages and in MH-S cells.

Figure 4

(A) Adam17 transcript levels were measured by qRT-PCR from RNA isolated from primary alveolar macrophages of wild-type TK(+/+) and Ron TK(−/−) mice. Data is expressed as the mean ± the standard deviation and is representative of several independent experiments. Expression was normalized to an internal control as described in the Materials and Methods section. (B) Western analysis of Adam17 protein levels from alveolar macrophages isolated from wild type TK(+/+) and Ron TK(−/−) mice. Five µg of total cell lysates were loaded per lane with Actin serving as a loading control. (C) Western analysis of Adam17 protein levels from MH-S cell lysates. The murine prostate cancer cell line, TRAMP-C1, was used as a positive control for Adam17 expression and Actin expression is provided as a loading control.

HHS Vulnerability Disclosure